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SCHILLER AG

CH-MF-000012722 · Switzerland · Baar

SCHILLER AG is registered in the European database on medical devices as a manufacturer, with 80 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIa53
Class IIb27

Most frequent device types declared: ARGUS LifePoint, ARGUS PB-3000, ARGUS PRO LifeCare 2, BPCV14XS - Velcro cuff XS, CS-3 Charging Station.

Among these devices, 1 are declared reusable, 49 active, 13 with a measuring function.

Authorised representative in the Union: SCHILLER Medizintechnik GmbH.

Devices declared under this manufacturer

Showing 12 of 80 declared devices.

Catalogue references include 2.120065, 3.900100, 3.900491, 3.921003, 3.921007, 3.921031.

European nomenclature codes declared: Z1203020299, Z1203020302, Z12050301, Z12050380, Z12030503, Z12050403.

United States market access

FDA establishment registerRegistered with FDA
Matched entrySCHILLER AG (CH) · FDA 8030978
Devices in EUDAMED80
Country of registrationSwitzerland

Device-level evidence

Devices with a numeric GTIN80
Found in the U.S. device database29
Share36.2 %

Canadian market access

Health Canada licence listingLicensed in Canada
Matched entrySCHILLER AG

What it holds in Canada

Licences on record22
Currently active0
Class 2 devices18
Class 3 devices4
First licensed2003-12-23

Licence types: System (14), Device Family (3), Single Device (3), Device Group (2).

Licensed under: PC SPIROMETRY SYSTEM, CARDIOVIT FT-1, PB-1000/2000, DIAGNOSTIC STATION DS-20, CARDIOVIT AT-102 G2, CARDIOVIT AT-1 G2.

North American profile: Both markets. SCHILLER AG is registered in both the United States and Canada.

Notified body certificates

CertificateStatusExpiry
G10 041505 0132issued2026-11-11

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